Canonical Allele Identifier: CA2760283918

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291470_6291471insACA , CM000666.2:g.6291470_6291471insACA	GRCh38
NC_000004.11:g.6293197_6293198insACA , CM000666.1:g.6293197_6293198insACA	GRCh37
NC_000004.10:g.6344098_6344099insACA	NCBI36
NG_011700.1:g.26621_26622insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+103_631+104insACA	ENSP00000507852.1:n.631+103_631+104insACA
ENST00000683395.1:c.608+116_608+117insACA
ENST00000684087.1:c.631+103_631+104insACA	ENSP00000506978.1:n.631+103_631+104insACA
ENST00000684700.1:c.*29_*30insACA	ENSP00000507806.1:n.*29_*30insACA
ENST00000506362.2:c.382+103_382+104insACA	ENSP00000424103.2:n.382+103_382+104insACA
ENST00000673642.1:c.430+103_430+104insACA	ENSP00000501242.1:n.430+103_430+104insACA
ENST00000673991.1:c.631+103_631+104insACA	ENSP00000501033.1:n.631+103_631+104insACA
ENST00000226760.5:c.631+103_631+104insACA MANE Select	ENSP00000226760.1:n.631+103_631+104insACA
ENST00000503569.5:c.631+103_631+104insACA	ENSP00000423337.1:n.631+103_631+104insACA
ENST00000506362.1:c.228+103_228+104insACA
ENST00000507765.1:n.816+103_816+104insACA
NM_001145853.1:c.631+103_631+104insACA	NP_001139325.1:n.631+103_631+104insACA
NM_006005.3:c.631+103_631+104insACA MANE Select	NP_005996.2:n.631+103_631+104insACA
XM_017008586.1:c.640+103_640+104insACA	XP_016864075.1:n.640+103_640+104insACA